JPH07173621A - Sintered target material for sputtering capable of high-speed film formation - Google Patents
Sintered target material for sputtering capable of high-speed film formationInfo
- Publication number
- JPH07173621A JPH07173621A JP32269693A JP32269693A JPH07173621A JP H07173621 A JPH07173621 A JP H07173621A JP 32269693 A JP32269693 A JP 32269693A JP 32269693 A JP32269693 A JP 32269693A JP H07173621 A JPH07173621 A JP H07173621A
- Authority
- JP
- Japan
- Prior art keywords
- target material
- sputtering
- film formation
- sintered
- bsto
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Landscapes
- Physical Vapour Deposition (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】この発明はSrTiO3 やBaT
iO3 、さらに(Sr、Ba)TiO3 の組成式で表さ
れるBSTO薄膜をスパッタリング法により形成するの
に用いられる焼結ターゲット材に関するものである。This invention relates to SrTiO 3 and BaT
The present invention relates to a sintering target material used for forming a BSTO thin film represented by a composition formula of iO 3 and (Sr, Ba) TiO 3 by a sputtering method.
【0002】[0002]
【従来の技術】従来、一般的に、赤外線センサー、圧電
フィルター、圧電振動子、レーザー変調素子、光シャッ
ター、半導体メモリー、薄膜コンデンサーなどの構成要
素として、SrTiO3 、BaTiO3 、および(S
r、Ba)TiO3 の組成式で表されるBSTO薄膜が
使用されていることは良く知られるとおりである。ま
た、上記BSTO薄膜をスパッタリング法により形成す
るのに用いられるターゲット材としては、特に酸素欠陥
を形成することにより導電性を高めて直流スパッタリン
グでの成膜を可能ならしめ、もって速い速度での成膜を
行うことができるBa X Sr1-X TiO3-Y で表される
ターゲット材が用いられていることも知られている。2. Description of the Related Art Conventionally, infrared sensors and piezoelectrics are generally used.
Filter, piezoelectric vibrator, laser modulator, optical shutter
Components, semiconductor memory, thin film capacitors, etc.
As a base, SrTiO3, BaTiO3, And (S
r, Ba) TiO3BSTO thin film represented by the composition formula
It is well known that it is used. Well
In addition, the above BSTO thin film is formed by the sputtering method.
The target material used to
The DC sputter phosphorus is formed by increasing the conductivity.
Film formation at high speed, and thus at high speed
Ba that can be done XSr1-XTiO3-YRepresented by
It is also known that target materials are used.
【0003】[0003]
【発明が解決しようとする課題】一方、近年のスパッタ
リング技術の進歩はめざましく、これに伴いより速い速
度での成膜が可能となったが、上記の一般式BaX Sr
1-X TiO3-Y の組成を有する従来焼結ターゲット(以
下酸素欠陥型焼結ターゲットという)の場合、成膜速度
をより一段と高めるために印可出力を高くすると割れが
発生し易くなることから、より高速での成膜は不可能で
あり、高々15nm/分程度の速度での成膜を行うこと
しかできないのが現状である。On the other hand, the recent advances in sputtering technology have enabled remarkable film formation at higher speeds, but the above general formula Ba X Sr is used.
In the case of a conventional sintered target having a composition of 1-X TiO 3 -Y (hereinafter referred to as an oxygen deficient sintered target), cracking is likely to occur when the applied output is increased in order to further increase the film formation rate. At present, it is impossible to form a film at a higher speed, and at present, only a film can be formed at a speed of about 15 nm / min.
【0004】[0004]
【問題を解決するための手段】そこで、本発明者等は上
述のような観点から、上記の従来酸素欠陥型焼結ターゲ
ットに着目し、これを用いてのより速い速度での成膜を
可能ならしめるべく研究を行った結果、上記従来酸素欠
陥型焼結ターゲットは、アルカリ金属不純物として50
〜200ppmを含有するが、このアルカリ金属不純物
の含有量を10ppm以下に低減すると、より一段と導
電性が上昇し、直流スパッタリングで、かつ、高出力印
可での成膜を行っても割れが発生しなくなり、速い速度
での成膜が可能になるという研究結果を得たのである。
この発明は、上記の研究結果に基づいてなされたもの
であって、酸素欠陥のある一般式BaX Sr1-X TiO
3- Y で表されるBSTO薄膜形成用スパッタリング焼結
ターゲット材において、アルカリ金属不純物を10pp
m以下とすることにより速い成膜速度でのBSTO薄膜
の形成を可能ならしめた点に特徴を有するものである。Therefore, from the viewpoints described above, the present inventors have focused their attention on the above-mentioned conventional oxygen-defect-type sintering target, and can use this to form a film at a higher speed. As a result of conducting a study to make it smooth, the conventional oxygen-defective sintering target described above has an alkali metal impurity content of 50%.
The content of the alkali metal impurities is reduced to 10 ppm or less, but the conductivity is further increased, and cracking occurs even when the film is formed by DC sputtering and high power application. That is, the research result was obtained that the film could be deposited at a high speed.
The present invention was made based on the above-mentioned research results, and has the general formula of Ba X Sr 1-X TiO 2 having oxygen defects.
In the sputtering sintered target material for BSTO thin film formation represented by 3- Y , alkali metal impurities of 10 pp
It is characterized in that the BSTO thin film can be formed at a high film forming rate by setting the thickness to m or less.
【0005】なお、この発明のスパッタリング用焼結タ
ーゲット材において、アルカリ金属不純物の含有量を1
0ppm以下と限定したのは、その含有量が10ppm
を越えた範囲では抵抗率は一定であるが、10ppmよ
りも少なくなると抵抗率が低くなり始め、高出力印可時
の割れ発生が著しく抑制されるようになるという理由に
よるものである。In the sintering target material for sputtering of the present invention, the content of alkali metal impurities is 1
Limited to 0 ppm or less, the content is 10 ppm
The reason is that the resistivity is constant in the range exceeding 10 .mu.m, but when it is less than 10 ppm, the resistivity starts to decrease and the cracking at the time of high output application is remarkably suppressed.
【0006】また、この発明のスパッタリング用焼結タ
ーゲット材は、BSTOの構成元素であるBa、Sr、
Tiの各化合物を再結晶、蒸留、昇華法等によりそれぞ
れ高純度化し、所定の組成比となるように混合、焼成、
焼結することによって得られる。The sintered target material for sputtering according to the present invention comprises Ba, Sr, which is a constituent element of BSTO,
Each compound of Ti is highly purified by recrystallization, distillation, sublimation method, etc., and is mixed and fired so as to have a predetermined composition ratio.
Obtained by sintering.
【0007】[0007]
【実施例】つぎに、この発明の焼結ターゲット材を実施
例により具体的に説明する。再結晶法によって高純度化
を行った酢酸Baと酢酸Srをそれぞれ熱分解すること
で高純度BaO、SrO粉末を得た。また、蒸留法によ
って高純度化を行ったチタニウムテトライソプロポキシ
ドをIPAに溶かし、水を加えて加水分解し、熱処理を
行って高純度TiO2 粉末を得た。これら粉末をそれぞ
れ所定の割合で混合し、熱処理を行ってペロブスカイト
型結晶構造を有したBSTO粉末を得た。更にこの粉末
を酸素欠陥を形成するために窒素気流中で1200℃で
2時間熱処理を行い、導電性の粉末を得た。この粉末を
用いてホットプレス法で、表1に示した組成を有する直
径200mmのスパッタリング用焼結ターゲット材(以
下、本発明ターゲット材という)1〜5を作製した。EXAMPLES Next, the sintering target material of the present invention will be specifically described by way of examples. Highly purified BaO and SrO powders were obtained by thermally decomposing highly purified Ba acetate and Sr acetate by the recrystallization method. Further, titanium tetraisopropoxide highly purified by the distillation method was dissolved in IPA, water was added to hydrolyze the mixture, and heat treatment was performed to obtain high purity TiO 2 powder. These powders were mixed at a predetermined ratio and heat-treated to obtain BSTO powder having a perovskite type crystal structure. Further, this powder was heat-treated at 1200 ° C. for 2 hours in a nitrogen stream in order to form oxygen defects, and a conductive powder was obtained. Using this powder, sintered target materials for sputtering having a composition shown in Table 1 and having a diameter of 200 mm (hereinafter, referred to as target material of the present invention) 1 to 5 were prepared by using the powder.
【0008】なお、比較の目的で、原料粉末として市販
のBaO、SrO、TiO2 粉末を使用し上記と同様に
して表2に示したスパッタリング用焼結ターゲット材
(以下、従来ターゲット材という)1〜5を作製した。
これらターゲット材のアルカリ金属含有量、焼結密度、
抵抗率を表3に示す。また、これらターゲット材を使用
して表4に示す条件でスパッタリングを行い成膜し、こ
の時の成膜速度を測定し、この測定結果を表5に示し
た。For comparison purposes, commercially available BaO, SrO, and TiO 2 powders were used as raw material powders and the sintering target materials for sputtering (hereinafter referred to as conventional target materials) 1 shown in Table 2 in the same manner as described above. ~ 5 were produced.
Alkali metal content of these target materials, sintered density,
The resistivity is shown in Table 3. Further, using these target materials, sputtering was performed under the conditions shown in Table 4 to form a film, and the film formation rate at this time was measured. The measurement results are shown in Table 5.
【0009】[0009]
【表1】 [Table 1]
【0010】[0010]
【表2】 [Table 2]
【0011】[0011]
【表3】 [Table 3]
【0012】[0012]
【表4】 [Table 4]
【0013】[0013]
【表5】 [Table 5]
【0014】[0014]
【発明の効果】以上のようにこの発明の焼結ターゲット
材1〜5は、スパッタ電力密度を上げていってもターゲ
ット材に割れがなく、よりいっそうの高速成膜が可能で
あるのに対して、従来ターゲット材1〜5には、すべて
に割れが発生し、実用に供することができないことが明
らかである。As described above, in the sintered target materials 1 to 5 of the present invention, even if the sputtering power density is increased, the target material does not crack, and higher speed film formation is possible. It is clear that the conventional target materials 1 to 5 are all cracked and cannot be put to practical use.
Claims (1)
O3-Y で表されるBSTO薄膜 形成用スパッタリング
焼結ターゲット材において、アルカリ金属不純物量を1
0ppm以下としたことを特徴とする高速成膜が可能な
スパッタリング用焼結ターゲット材。1. A general formula Ba X Sr 1-X Ti with oxygen defects.
In the sputtering sintering target material for BSTO thin film formation represented by O 3-Y , the amount of alkali metal impurities is set to 1
A sintered target material for sputtering capable of high-speed film formation, which has a content of 0 ppm or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32269693A JPH07173621A (en) | 1993-12-21 | 1993-12-21 | Sintered target material for sputtering capable of high-speed film formation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32269693A JPH07173621A (en) | 1993-12-21 | 1993-12-21 | Sintered target material for sputtering capable of high-speed film formation |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH07173621A true JPH07173621A (en) | 1995-07-11 |
Family
ID=18146597
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP32269693A Pending JPH07173621A (en) | 1993-12-21 | 1993-12-21 | Sintered target material for sputtering capable of high-speed film formation |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH07173621A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6245203B1 (en) | 1997-10-01 | 2001-06-12 | Japan Energy Corporation | BaxSr1-xTiO3-y target materials for sputtering |
WO2013150831A1 (en) * | 2012-04-02 | 2013-10-10 | ソニー株式会社 | Sputtering target, sputtering target manufacturing method, barium titanate thin film manufacturing method, and thin film capacitor manufacturing method |
-
1993
- 1993-12-21 JP JP32269693A patent/JPH07173621A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6245203B1 (en) | 1997-10-01 | 2001-06-12 | Japan Energy Corporation | BaxSr1-xTiO3-y target materials for sputtering |
WO2013150831A1 (en) * | 2012-04-02 | 2013-10-10 | ソニー株式会社 | Sputtering target, sputtering target manufacturing method, barium titanate thin film manufacturing method, and thin film capacitor manufacturing method |
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Legal Events
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A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20020115 |